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Showing results (341-350 of 580) with videos related to

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Kidney International|February 14, 1998
Hereditary nephropathic systemic amyloidosis caused by a novel variant apolipoprotein A-IM R Persey, D R Booth, S E Booth, et al.
Transplantation|May 15, 2001
Clinical and biochemical outcome of hepatorenal transplantation for hereditary systemic amyloidosis associated with apolipoprotein AI Gly26ArgJ D Gillmore, A J Stangou, G A Tennent, et al.
The Journal of Pathology|October 24, 2007
Disease-associated prion protein is not detectable in human systemic amyloid depositsG A Tennent, M W Head, M Bishop, et al.
Arthritis Research & Therapy|December 14, 2011
Sustained remission of symptoms and improved health-related quality of life in patients with cryopyrin-associated periodic syndrome treated with canakinumab: results of a double-blind placebo-controlled randomized withdrawal studyIsabelle Koné-Paut, Helen J Lachmann, Jasmin B Kuemmerle-Deschner, et al.
Arthritis and Rheumatism|January 3, 2013
AA amyloidosis complicating the hereditary periodic fever syndromesThirusha Lane, Jutta M Loeffler, Dorota M Rowczenio, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|March 8, 2014
Novel gelsolin variant as the cause of nephrotic syndrome and renal amyloidosis in a large kindredYvonne A Efebera, Amy Sturm, Elizabeth C Baack, et al.
Journal of Neuromuscular Diseases|March 12, 2019
Spinal Stenosis in Familial Transthyretin AmyloidosisA S Carr, S Shah, D Choi, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 7, 1994
Human serum amyloid P component is an invariant constituent of amyloid deposits and has a uniquely homogeneous glycostructureM B Pepys, T W Rademacher, S Amatayakul-Chantler, et al.
Rheumatology (Oxford, England)|January 13, 2006
Clinical and subclinical inflammation in patients with familial Mediterranean fever and in heterozygous carriers of MEFV mutationsH J Lachmann, B Sengül, T U Yavuzşen, et al.
Arthritis and Rheumatism|January 1, 2008
Abnormal tumor necrosis factor receptor I cell surface expression and NF-kappaB activation in tumor necrosis factor receptor-associated periodic syndromeBelinda Nedjai, Graham A Hitman, Nasim Yousaf, et al.
Pageof 58

Showing results (341-350 of 580) with videos related to

Sort By:
Pageof 58
Kidney International|February 14, 1998
Hereditary nephropathic systemic amyloidosis caused by a novel variant apolipoprotein A-IM R Persey, D R Booth, S E Booth, et al.
Transplantation|May 15, 2001
Clinical and biochemical outcome of hepatorenal transplantation for hereditary systemic amyloidosis associated with apolipoprotein AI Gly26ArgJ D Gillmore, A J Stangou, G A Tennent, et al.
The Journal of Pathology|October 24, 2007
Disease-associated prion protein is not detectable in human systemic amyloid depositsG A Tennent, M W Head, M Bishop, et al.
Arthritis Research & Therapy|December 14, 2011
Sustained remission of symptoms and improved health-related quality of life in patients with cryopyrin-associated periodic syndrome treated with canakinumab: results of a double-blind placebo-controlled randomized withdrawal studyIsabelle Koné-Paut, Helen J Lachmann, Jasmin B Kuemmerle-Deschner, et al.
Arthritis and Rheumatism|January 3, 2013
AA amyloidosis complicating the hereditary periodic fever syndromesThirusha Lane, Jutta M Loeffler, Dorota M Rowczenio, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|March 8, 2014
Novel gelsolin variant as the cause of nephrotic syndrome and renal amyloidosis in a large kindredYvonne A Efebera, Amy Sturm, Elizabeth C Baack, et al.
Journal of Neuromuscular Diseases|March 12, 2019
Spinal Stenosis in Familial Transthyretin AmyloidosisA S Carr, S Shah, D Choi, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 7, 1994
Human serum amyloid P component is an invariant constituent of amyloid deposits and has a uniquely homogeneous glycostructureM B Pepys, T W Rademacher, S Amatayakul-Chantler, et al.
Rheumatology (Oxford, England)|January 13, 2006
Clinical and subclinical inflammation in patients with familial Mediterranean fever and in heterozygous carriers of MEFV mutationsH J Lachmann, B Sengül, T U Yavuzşen, et al.
Arthritis and Rheumatism|January 1, 2008
Abnormal tumor necrosis factor receptor I cell surface expression and NF-kappaB activation in tumor necrosis factor receptor-associated periodic syndromeBelinda Nedjai, Graham A Hitman, Nasim Yousaf, et al.
Pageof 58